Tag | Content |
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EnhancerAtlas ID | HS040-34719 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr9:95320820-95321530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr9:95321160-95321175 | TCTGCTGAGTCATGC | - | 7.23 | Nfe2l2 | MA0150.2 | chr9:95321162-95321177 | TGCTGAGTCATGCAG | - | 7.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGTGGCAGAG GGTGCAATGG ACACCATGAG GGTCCTTAGC TTTGGTGATT TAATTATCTA 60 TTTTTGTGCT GGTTGGCCTC CTGTCAAGAG GTGATGCTTC CTGGAAGGCA TCAGCTGTAG 120 TAGAGTGGAA AGGGACCAGC AGTAGGCGGG GTCCTAGAAT TCCCAAGACT ATAGGCCCTT 180 TGTCTTCAGC TACCAGGGTG GATAGGAAAG GACCATCAGG TGGGGACAGG GCTAGGTGTG 240 TTTGAGCTCT CCTTGGGTGG GTCTTGCTGC GGCTGCTGTG GGGGATGGGG TGAGATTCCC 300 AGGTCACTGG AGTTGTATAC CTAGGAGGAT TATGGCTTCC TCTGCTGAGT CATGCAGGTT 360 GTCAGGGAAG TTGGGGAAAG CCGGCAGTCA CAGGCCTCAC CCAGTTCCCA CGCAAACTGC 420 AAACTGAAGG GCAGTTCCCC CGCCACCCAA CAGCCCCAAG TCTGTTTCCA AGCAGAGGGC 480 AAGAGGGGCT TGAAAACTTA CCCGAGGCTG TCCACCTCCC AGCTGCCAAA GAAAAGGGCT 540 CTTCCCCCGC CTCTGAAGTC TGCACACTGG ATTCGCGCCC TCCCCCAGTT CTGGCCAGGA 600 GGCTTCTTGT CCCGTTCAAA TTGTTACAAA GTTCGGCTAG AGAATTCATT CTCCCTGTGG 660 AGTTTTACCC CTGCTCCTCT GGCCGCCCTC CCGATGGATC CCTGTGGTGT 710
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